美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
50090-6635-0	50090-6635	HUMAN PRESCRIPTION DRUG	Potassium Chloride	potassium chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230825	N/A	ANDA	ANDA204662	A-S Medication Solutions	POTASSIUM CHLORIDE	10 meq/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6635-0)
0378-4561-05	0378-4561	HUMAN PRESCRIPTION DRUG	Potassium Chloride	potassium chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20161109	N/A	ANDA	ANDA204662	Mylan Pharmaceuticals Inc.	POTASSIUM CHLORIDE	10 meq/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-4561-05)
0378-4561-77	0378-4561	HUMAN PRESCRIPTION DRUG	Potassium Chloride	potassium chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20161109	N/A	ANDA	ANDA204662	Mylan Pharmaceuticals Inc.	POTASSIUM CHLORIDE	10 meq/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-4561-77)
0378-4560-05	0378-4560	HUMAN PRESCRIPTION DRUG	Potassium Chloride	potassium chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20161109	N/A	ANDA	ANDA204662	Mylan Pharmaceuticals Inc.	POTASSIUM CHLORIDE	8 meq/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-4560-05)
0378-4560-77	0378-4560	HUMAN PRESCRIPTION DRUG	Potassium Chloride	potassium chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20161109	N/A	ANDA	ANDA204662	Mylan Pharmaceuticals Inc.	POTASSIUM CHLORIDE	8 meq/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-4560-77)